Identifying Phase-Amplitude Coupling in Cyclic Alternating Pattern using Masking Signals

被引:22
|
作者
Yeh, Chien-Hung [1 ]
Shi, Wenbin [2 ]
机构
[1] Chang Gung Mem Hosp & Univ, Dept Neurol, Taoyuan, Taiwan
[2] Tsinghua Univ, Dept Hydraul Engn, State Key Lab Hydrosci & Engn, Beijing, Peoples R China
来源
SCIENTIFIC REPORTS | 2018年 / 8卷
基金
中国博士后科学基金;
关键词
EMPIRICAL MODE DECOMPOSITION; SLEEP; CAP; NONSTATIONARY; OSCILLATIONS; MODULATION; ALGORITHMS; COMPONENTS;
D O I
10.1038/s41598-018-21013-9
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Judiciously classifying phase-A subtypes in cyclic alternating pattern (CAP) is critical for investigating sleep dynamics. Phase-amplitude coupling (PAC), one of the representative forms of neural rhythmic interaction, is defined as the amplitude of high-frequency activities modulated by the phase of low-frequency oscillations. To examine PACs under more or less synchronized conditions, we propose a nonlinear approach, named the masking phase-amplitude coupling (MPAC), to quantify physiological interactions between high (alpha/low beta) and low (delta) frequency bands. The results reveal that the coupling intensity is generally the highest in subtype A1 and lowest in A3. MPACs among various physiological conditions/disorders (p < 0.0001) and sleep stages (p < 0.0001 except S4) are tested. MPACs are found significantly stronger in light sleep than deep sleep (p < 0.0001). Physiological conditions/disorders show similar order in MPACs. Phase-amplitude dependence between delta and alpha/low beta oscillations are examined as well. delta phase tent to phase-locked to alpha/low beta amplitude in subtype A1 more than the rest. These results suggest that an elevated delta-alpha/low beta MPACs can reflect some synchronization in CAP. Therefore, MPAC can be a potential tool to investigate neural interactions between different time scales, and delta-alpha/low beta MPAC can serve as a feasible biomarker for sleep microstructure.
引用
收藏
页数:9
相关论文
共 50 条
  • [1] Identifying Phase-Amplitude Coupling in Cyclic Alternating Pattern using Masking Signals
    Chien-Hung Yeh
    Wenbin Shi
    [J]. Scientific Reports, 8
  • [2] Multivariate Phase-Amplitude Cross-Frequency Coupling in Neurophysiological Signals
    Canolty, Ryan T.
    Cadieu, Charles F.
    Koepsell, Kilian
    Knight, Robert T.
    Carmena, Jose M.
    [J]. IEEE TRANSACTIONS ON BIOMEDICAL ENGINEERING, 2012, 59 (01) : 8 - 11
  • [3] Multitaper estimates of phase-amplitude coupling
    Lepage, Kyle Q.
    Fleming, Cavan N.
    Witcher, Mark
    Vijayan, Sujith
    [J]. JOURNAL OF NEURAL ENGINEERING, 2021, 18 (05)
  • [4] Realtime phase-amplitude coupling analysis of micro electrode recorded brain signals
    Lu, David Chao-Chia
    Boulay, Chadwick
    Chan, Adrian D. C.
    Sachs, Adam J.
    [J]. PLOS ONE, 2018, 13 (09):
  • [5] A Precise Annotation of Phase-Amplitude Coupling Intensity
    Cheng, Ning
    Li, Qun
    Xu, Xiaxia
    Zhang, Tao
    [J]. PLOS ONE, 2016, 11 (10):
  • [6] A neural mass model of phase-amplitude coupling
    Chehelcheraghi, Mojtaba
    Nakatani, Chie
    Steur, Erik
    van Leeuwen, Cees
    [J]. BIOLOGICAL CYBERNETICS, 2016, 110 (2-3) : 171 - 192
  • [7] Phase-Amplitude Coupling in Spontaneous Mouse Behavior
    Thengone, Daniel
    Gagnidze, Khatuna
    Pfaff, Donald
    Proekt, Alex
    [J]. PLOS ONE, 2016, 11 (09):
  • [8] Thalamocortical control of propofol phase-amplitude coupling
    Soplata, Austin E.
    McCarthy, Michelle M.
    Sherfey, Jason
    Lee, Shane
    Purdon, Patrick L.
    Brown, Emery N.
    Kopell, Nancy
    [J]. PLOS COMPUTATIONAL BIOLOGY, 2017, 13 (12)
  • [9] Phase-amplitude coupling in neuronal oscillator networks
    Qin, Yuzhen
    Menara, Tommaso
    Bassett, Danielle S.
    Pasqualetti, Fabio
    [J]. PHYSICAL REVIEW RESEARCH, 2021, 3 (02):
  • [10] Empirical analysis of phase-amplitude coupling approaches
    Caiola, Michael
    Devergnas, Annaelle
    Holmes, Mark H.
    Wichmann, Thomas
    [J]. PLOS ONE, 2019, 14 (07):